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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Cyclohexanemethanamine, 1-(4-morpholinyl)-

NCC1(CCCCC1)N1CCOCC1 Request for Quotation
Chemical Name: Cyclohexanemethanamine, 1-(4-morpholinyl)-
CAS Number: 64269-03-0
Product Number: AG00EA27(AGN-PC-0KPXYR)
Synonyms:
MDL No:
Molecular Formula: C11H22N2O
Molecular Weight: 198.3052

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
198.31g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
198.173g/mol
Monoisotopic Mass:
198.173g/mol
Topological Polar Surface Area:
38.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
172
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3259
Hazard Statements:
H314-H318
Precautionary Statements:
P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (1-Morpholinocyclohexyl)methanamine in chemical synthesis lies in its versatility as a building block for various organic compounds. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structure and reactivity. (1-Morpholinocyclohexyl)methanamine can participate in a variety of reactions, such as nucleophilic substitution, reductive amination, and cyclization, offering a wide range of synthetic pathways for the production of complex molecules. Its cyclic morphology, incorporating a morpholine ring and a cyclohexyl group, imparts specific stereochemical and steric properties to the resulting products. As a crucial component in the toolbox of organic chemists, (1-Morpholinocyclohexyl)methanamine plays a vital role in the strategic design and synthesis of functional molecules for diverse applications.